Garnier Skin Naturals Lift SPF 15 Day

Manufacturer
L'Oreal USA Products Inc
Effective date
2018-12-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:11:54

Label at a glance#

ProductGarnier Skin Naturals Lift SPF 15 Day
Active ingredientEnsulizole, Octinoxate
Label structure8 sections

Dosage and administration

Apply every morning before sun exposure with light circular movements, moving from the center of your face outwards, and from the base to the top of your neck.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ensulizole 1.7%; Octinoxate 7.5%

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

AVOID CONTACT WITH THE EYES. 

Stop use and consult a doctor if

OTC - STOP USE SECTION

SIGNS OF IRRITATION DEVELOPS OR INCREASES.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply every morning before sun exposure with light circular movements, moving from the center of your face outwards, and from the base to the top of your neck.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, dimethicone, glycerin, myristyl myristate, stearic acid, triethanolamine, palmitic acid, ammonium polyacryloyldimethyl taurate, ci 77891, peg-100 stearate, glyceryl stearate, stearyl alcohol, cera alba, cetyl alcohol, caprylyl glycol, paraffin, peg-20 stearate, argania spinosa, retinyl linoleate, acrylates copolymer, disodium edta, phenoxyethanol, hydrolyzed rice protein, glycine soja oil, carbomer, cera carnauba, tocopherol, capryloyl salicylic acid, alumina, sodium cocoyl glutamate, zingiber officinale root extract, methylparaben, ethylparaben, benzyl alcohol, linalool, citral, limonene, coumarin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
EnsulizoleACTIVE INGREDIENT9YQ9DI1W422
OctinoxateACTIVE INGREDIENT4Y5P7MUD512
EnsulizoleACTIVE MOIETY9YQ9DI1W422
OctinoxateACTIVE MOIETY4Y5P7MUD512

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-67149967-671-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c2f5c1d5-171b-433a-8c22-c408e16e2be09470c7d8-281b-4e24-912f-d88aced33ac52018-12-26WarningsExact identifier
spl id: c2f5c1d5-171b-433a-8c22-c408e16e2be0
spl set id: 9470c7d8-281b-4e24-912f-d88aced33ac5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.